Group Regulatory Affairs Specialist Class II
KI-Beschreibung
In this role, you will navigate the complex regulatory landscape, ensuring product compliance from development to post-market. You will collaborate with cross-functional teams, provide guidance on regulatory requirements, and stay updated on scientific advances that shape healthcare regulations.
Anforderungen
3 Jahre- •Master’s degree in science or equivalent experience
- •Minimum of 3 years experience in Regulatory Affairs for medical devices
- •In-depth knowledge of US and Canada regulations for medical devices